Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter13: Substitution
Section: Chapter Questions
Problem 51CTQ
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Question
![Mechanistically, the addition of HCl to this alkene is regioselective and gives only one product because:](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F34087137-9349-47df-b35e-0681e4892fc3%2Fcf345a06-daad-4b09-b127-53d689b12dd8%2F7wupqn_processed.jpeg&w=3840&q=75)
Transcribed Image Text:Mechanistically, the addition of HCl to this alkene is regioselective and gives only one product because:
![Multiple Choice
one possible carbocation intermediate reacts faster than the other.
the most stable alkyl halide product is preferred.
the halogen adds to the more substituted carbon.
one possible carbocation intermediate is more stable than the other.
steric crowding favours only one product.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F34087137-9349-47df-b35e-0681e4892fc3%2Fcf345a06-daad-4b09-b127-53d689b12dd8%2F48i9udc_processed.jpeg&w=3840&q=75)
Transcribed Image Text:Multiple Choice
one possible carbocation intermediate reacts faster than the other.
the most stable alkyl halide product is preferred.
the halogen adds to the more substituted carbon.
one possible carbocation intermediate is more stable than the other.
steric crowding favours only one product.
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